# Adalimumab-Induced Pneumocystis jirovecii Pneumonitis (PCP) Misdiagnosed As Methotrexate-Induced Pneumonitis

**Authors:** Shayekh Ferdoush, Abir Aijaz, Shovan Rahman, Mustain Jawad, Muhammad Hamid

PMC · DOI: 10.7759/cureus.88084 · 2025-07-16

## TL;DR

A patient with rheumatoid arthritis was misdiagnosed with methotrexate-induced lung disease but later found to have a rare fungal infection.

## Contribution

This case highlights the diagnostic challenge of distinguishing PCP from drug-induced pneumonitis in immunocompromised patients.

## Key findings

- PCP was initially misdiagnosed as methotrexate-induced pneumonitis in a patient with rheumatoid arthritis.
- PCR testing of bronchoalveolar lavage confirmed the presence of Pneumocystis jirovecii.

## Abstract

Pneumocystis jirovecii pneumonia (PCP), a life-threatening opportunistic infection, occasionally mimics drug-induced pneumonitis, posing a diagnostic challenge in immunocompromised patients (such as those with rheumatoid arthritis, RA, on immunosuppressive therapy). We present a 46-year-old woman with seropositive RA treated with long-term methotrexate and recently initiated on adalimumab, who presented with progressive dyspnea, dry cough, and low-grade fever. Imaging revealed bilateral interstitial and ground-glass opacities, initially attributed to methotrexate-induced pneumonitis (MTX-IP). Methotrexate was discontinued, and corticosteroids were started, but clinical deterioration ensued. Bronchoalveolar lavage with polymerase chain reaction (PCR) confirmed PCP, leading to a revised diagnosis. The patient responded well to trimethoprim-sulfamethoxazole and corticosteroids, with full recovery and resolution of pulmonary findings. This case highlights the importance of distinguishing PCP from drug-induced lung toxicity, particularly in patients receiving tumor necrosis factor-α inhibitors like adalimumab, which significantly increase susceptibility to opportunistic infections. MTX-IP usually occurs within the first year, whereas PCP may develop insidiously. Elevated lactate dehydrogenase levels and poor response to corticosteroids should prompt further investigation. Early use of diagnostic tools such as bronchoalveolar lavage with PCR is critical for timely diagnosis and treatment. Clinicians must maintain a high index of suspicion for PCP in RA patients with new pulmonary symptoms while on biologic therapy.

## Linked entities

- **Chemicals:** methotrexate (PubChem CID 4112), trimethoprim-sulfamethoxazole (PubChem CID 358641)
- **Diseases:** rheumatoid arthritis (MONDO:0008383), Pneumocystis jirovecii pneumonia (MONDO:0019121)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** PCP (MESH:D011020), opportunistic infection (MESH:D009894), fever (MESH:D005334), lung toxicity (MESH:D008171), RA (MESH:D001172), dyspnea (MESH:D004417), IP (MESH:D007184), Pneumonitis (MESH:D011014), opacities (MESH:D003318), dry cough (MESH:D003371), seropositive (MESH:D006679)
- **Chemicals:** MTX (MESH:D008727), Adalimumab (MESH:D000068879), trimethoprim-sulfamethoxazole (MESH:D015662)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12356243/full.md

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Source: https://tomesphere.com/paper/PMC12356243